Structure and acidity changes of the acid sites in ultra-stable Y zeolites of different cell sizes during the hydrothermal aging process were studied by solid-state nuclear magnetic resonance (NMR) combined with molecular probes. The experimental results demonstrated that, during the initial stage of hydrothermal aging, parts of the framework aluminum species were removed from the framework and formed five-coordinate extra-framework aluminum species. In the meanwhile, the five-coordinate extra-framework aluminum species migrated to the surface and formed poly-aluminum species, resulting in decreases of both Brønsted acid sites and Lewis acid sites. The acidity of ultra-stable Y zeolites changed considerably during the first 3 h of the aging process, and the change of Brønsted acid content was proportional to the unit cell dimension of the fresh zeolites agent. With the increase of aging time, the aluminum distribution tended to become stable, with little further changes in the amounts of Brønsted acid and Lewis acid sites. The synergy between Brønsted/Lewis acids in the ultra-stable Y zeolites existed during the entire aging process, resulting in a stably enhanced acidity for the Brønsted acid sites.
GAO Xiu-zhi
,
ZHANG Yi
,
WANG Xiu-mei
,
ZHANG Zhi-hua
,
XU Guang-tong
. Structure and Acidity Changes in Ultra-Stable Y Zeolites During Hydrothermal Aging: A Solid-State NMR Spectroscopy Study[J]. Chinese Journal of Magnetic Resonance, 2020
, 37(1)
: 95
-103
.
DOI: 10.11938/cjmr20192745
[1] ARRIBAS J, CORMA A, FORNES V, et al. Influence of framework aluminum gradients on the catalytic activity of Y zeolites:Cracking of gas-oil on Y zeolites dealuminated by different procedures[J]. J Catal, 1987, 108(1):135-142.
[2] CORMA A, FORNES V, MARTINEZ A, et al. Influence of the method of dealumination of Y zeolites on its behaviour for cracking N-heptane and vacuum gas oil[J]. Stud Surf Sci Catal, 1988, 37(6):495-503.
[3] WILLIAMS B A, BABITZ S M, MILLER J T, et al. The roles of acid strength and pore diffusion in the enhanced cracking activity of steamed Y zeolites[J]. Appl Catal A:Gen, 1999, 177(2):161-175.
[4] CORMA A, FORNES V, MARTINEZ A, et al. Parameters in addition to the unit cell that determine the cracking activity and selectivity of dealuminated HY zeolites[J]. ACS Sym Ser, 1988, 368(368):542-554.
[5] XU B, BORDIGA S, PRINS R, et al. Effect of framework Si/Al ratio and extra-framework aluminum on the catalytic activity of Y zeolite[J]. Appl Catal A:Gen, 2007, 333(2):245-253.
[6] CORMA A, GRANDE M, FORNéS V, et al. Interaction of zeolite alumina with matrix silica in catalytic cracking catalysts[J]. Appl Catal, 1990, 66(1):45-57.
[7] WANG Q L, GIANNETTOG, GUISNET M. Dealumination of zeolites III. Effect of extra-framework aluminum species on the activity, selectivity, and stability of Y zeolites in n-heptane cracking[J]. J Catal, 1991, 130(2):471-482.
[8] LOEFFLER E, LOHSE U, PEUKER C H, et al. Study of different states of nonframework aluminum in hydrothermally dealuminated HZSM-5 zeolites using diffuse reflectance IR spectroscopy[J]. Zeolites, 1990, 10(4):266-271.
[9] MEYERSBL, FLEISCH TH, RAY G J, et al. Multitechnique characterization of dealuminatedmordenites[J]. J Catal, 1988, 110(1):82-95.
[10] GAO X Z, WANG X M, XU G T, et al. Insight into structureand acidity evolution mechanism of Y zeolites during hydrothermal aging[C]. Chinese zeolite conference, 2013.高秀枝, 王秀梅, 徐广通, 等. Y型分子筛水热老化过程中结构和酸性变化规律的研究[C]. 全国分子筛学术大会会议. 2013.
[11] GAO X Z, ZHANG Y, XU G T, et al. Insight into structure evolution mechanism of ultra-stable Y zeolites during hydrothermal aging[J]. Acta Petrolei Sinica, 2016, 32(2):357-363.高秀枝, 张翊, 徐广通, 等. 超稳Y分子筛水热老化过程中的结构变化规律[J]. 石油学报, 2016, 32(2):357-363.
[12] GAO X Z, ZHANG Y, WANG X M, et al. State of acidic center and acidity of dealuminated HY zeolites investigated by solid-state NMR spectroscopy[J].Acta Petrolei Sinica, 2012, 28(2):180-187.高秀枝, 张翊, 王秀梅, 等. 脱铝HY分子筛酸中心结构与酸性的固体NMR研究[J]. 石油学报, 2012, 28(2):180-187.
[13] YU Z W, AMOUREUX J P, DENG F, et al. Insights into the dealumination of zeolite HY revealed by sensitivity-enhanced 27Al DQ-MAS NMR spectroscopy at high field[J]. Angew Chem Int Ed, 2010, 49(46):8657-8661.
[14] LI S H,YE C H, DENG F, et al. Brønsted/Lewis acid synergy in dealuminated HY zeolite:A combined solid-state NMR and theoretical calculation study[J]. J Am Chem Soc, 2007, 129(36):11161-11171.
[15] HAW J F, NICHOLAS J B, XU T, et al. Physical organic chemistry of solid acids:Lessons from in situ NMR and theoretical chemistry[J]. Accounts Chem Res, 1996, 29(6):259-267.
[16] LUNSFORD J H, ROTHWEL W P. Acid sites in zeolite Y:A solid-state NMR and infrared study using trimethylphosphine as a probe molecule[J]. J Am Chem Soc, 1985, 107:1540.
[17] ZHANG Y, OLDFIELD E. 31P NMR chemical shifts in hypervalent oxyphosphoranes and polymeric orthophosphates[J]. J Phys Chem B, 2006, 110:579.
[18] ZHENG A, LIU S B, DENG F. 31P NMR chemical shifts of phosphorus probes as reliable and practical acidity scales for solid and liquid catalysts[J]. Chem Rev, 2017, 117(19):12475-12531.